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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565854Generated: October 26, 2026

tert-Butyldimethyl((4-nitrobenzyl)oxy)silane → 4-Aminobenzyloxy-tert-butyldimethylsilane

https://huagongshe.com/reaction/565854

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethyl((4-nitrobenzyl)oxy)silaneHCID 11065418—
SolventEthanolHCID 702—
Product4-Aminobenzyloxy-tert-butyldimethylsilaneHCID 1107547094.2%

Reaction Steps

In ethanol (80 ml) was dissolved tert-butyldimethyl-4-nitrobenzyloxysilane (16.5 g), and to the mixture was added dried 5% palladium on carbon (0.83 g). Under hydrogen atmosphere, the mixture was stirred at room temperature under atmospheric pressure for 7.5 hours. The palladium was filtered off, and the filtrate was concentrated. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1/4) to give 4-aminobenzyloxy-tert-butyldimethylsilane (13.8 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-146cb188867747b6912f13ae57baacf6
Source noteuspto-grants-2001_01